Chemiluminescence emission in cholesteric liquid crystalline core-shell microcapsules

Chemiluminescence behaviour in the core region of water/oil/water double emulsion droplets with cholesteric liquid crystalline (CLC) middle phase (CLC core-shell microcapsules) was demonstrated. We successfully fabricated CLC core-shell microcapsules containing an aqueous luminol solution as the inner phase using a microfluidic device, in which the helical axis of the CLC phase is normal to the surface. The CLC core-shell microcapsules proved to be a plausible candidate for highly sensitive H₂O₂ sensors because of the omnidirectional photonic structures of the CLC phase.Iwai Y., Kaji H., Uchida Y., et al. Chemiluminescence emission in cholesteric liquid crystalline core-shell microcapsules. Journal of Materials Chemistry C 2, 4904 (2014); https://doi.org/10.1039/c4tc00699b

VEGF(164)-mediated inflammation is required for pathological, but not physiological, ischemia-induced retinal neovascularization

Hypoxia-induced VEGF governs both physiological retinal vascular development and pathological retinal neovascularization. In the current paper, the mechanisms of physiological and pathological neovascularization are compared and contrasted. During pathological neovascularization, both the absolute and relative expression levels for VEGF(164) increased to a greater degree than during physiological neovascularization. Furthermore, extensive leukocyte adhesion was observed at the leading edge of pathological, but not physiological, neovascularization. When a VEGF(164)-specific neutralizing aptamer was administered, it potently suppressed the leukocyte adhesion and pathological neovascularization, whereas it had little or no effect on physiological neovascularization. In parallel experiments, genetically altered VEGF(164)-deficient (VEGF(120/188)) mice exhibited no difference in physiological neovascularization when compared with wild-type (VEGF(+/+)) controls. In contrast, administration of a VEGFk-1/Fc fusion protein, which blocks all VEGF isoforms, led to significant suppression of both pathological and physiological neovascularization. In addition, the targeted inactivation of monocyte lineage cells with clodronate-liposomes led to the suppression of pathological neovascularization. Conversely, the blockade of T lymphocyte-mediated immune responses with an anti-CD2 antibody exacerbated pathological neovascularization. These data highlight important molecular and cellular differences between physiological and pathological retinal neovascularization. During pathological neovascularization, VEGF(164) selectively induces inflammation and cellular immunity. These processes provide positive and negative angiogenic regulation, respectively. Together, new therapeutic approaches for selectively targeting pathological, but not physiological, retinal neovascularization are outlined

30S Beam Development and X-ray Bursts

Over the past three years, we have worked on developing a well-characterized 30S radioactive beam to be used in a future experiment aiming to directly measure the 30S(alpha,p) stellar reaction rate within the Gamow window of Type I X-ray bursts. The importance of the 30S(alpha,p) reaction to X-ray bursts is discussed. Given the astrophysical motivation, the successful results of and challenges involved in the production of a low-energy 30S beam are detailed. Finally, an overview of our future plans regarding this on-going project are presented.Comment: 7 pages, 2 figures, 5th European Summer School on Experimental Nuclear Astrophysics, Santa Tecla, Sicily, September 200

Atomic masses of intermediate-mass neutron-deficient nuclei with relative uncertainty down to 35-ppb via multireflection time-of-flight mass spectrograph

High-precision mass measurements of $^{63}$Cu, $^{64-66}$Zn, $^{65}$Ga, $^{65-67}$Ge, $^{67}$As, $^{78,81}$Br, $^{80}$Rb, and $^{79}$Sr were performed utilizing a multireflection time-of-flight mass spectrograph combined with the gas-filled recoil ion separator GARIS-II. In the case of $^{65}$Ga, a mass uncertainty of 2.1 keV, corresponding to a relative precision of $\delta m / m = 3.5\times10^{-8}$, was obtained and the mass value is in excellent agreement with the 2016 Atomic Mass Evaluation. For $^{67}$Ge and $^{81}$Br, where masses were previously deduced through indirect measurements, discrepancies with literature values were found. The feasibility of using this device for mass measurements of nuclides more neutron-deficient side, which have significant impact on the $rp$-process pathway, is discussed.Comment: 15 pages, 6 figures, 1 tabl

A Study of Sum Peak Method in Biological Substances by Using 111In

開始ページ、終了ページ: 冊子体のページ付

Decay Properties of 266^{266}Bh and 262^{262}Db Produced in the 248^{248}Cm + 23^{23}Na Reaction

Decay properties of an isotope $^{266}$Bh and its daughter nucleus $^{262}$Db produced by the $^{248}$Cm($^{23}$Na, 5\textit{n}) reaction were studied by using a gas-filled recoil separator coupled with a position-sensitive semiconductor detector. $^{266}$Bh was clearly identified from the correlation of the known nuclide, $^{262}$Db. The obtained decay properties of $^{266}$Bh and $^{262}$Db are consistent with those observed in the $^{278}$113 chain, which provided further confirmation of the discovery of $^{278}$113.Comment: Accepted for publication in J. Phys. Soc. JPN., to be published in Vol.78 No.

Structure of Polyelectrolytes in Poor Solvent

We present simulations on charged polymers in poor solvent. First we investigate in detail the dilute concentration range with and without imposed extension constraints. The resulting necklace polymer conformations are analyzed in detail. We find strong fluctuations in the number of pearls and their sizes leading only to small signatures in the form factor and the force-extension relation. The scaling of the peak in the structure factor with the monomer density shows a pertinent different behavior from good solvent chains.Comment: 7 pages, 5 figures. submitted to EP